照亮道路:可持续的无催化剂方法对吲哚的三氟甲基化

IF 2 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Nikita Gupta, Imtiaz Ahmed, Ajit Kumar Gupta, Kalpajyoti Dihingia, Dr. Biswajit Maiti, Dr. Vijay Kumar Das
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引用次数: 0

摘要

在这项研究中,我们报告了可见光诱导合成三氟甲基吲哚的创新进展。这种新方法不仅消除了对传统催化剂的需要,而且利用光子的能量选择性地将三氟甲基引入吲哚底物中。利用廉价,易于处理和无毒的朗格卢瓦试剂(CF3SO2Na)作为CF3源,与可见光和过氧化氢叔丁基(thbhp)一起,促进了吲哚的直接C─H三氟甲基化。通过密度泛函理论(DFT)在(U)B3LYP/ 6-31 ++G(d,p)/SMD/乙腈水平上的计算,预测了反应的机理途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Lighting the Path: A Sustainable Catalyst Free Approach Toward Trifluoromethylation of Indoles

Lighting the Path: A Sustainable Catalyst Free Approach Toward Trifluoromethylation of Indoles

In this study, we report an innovative development of a visible light-induced synthesis of trifluoromethyl indoles. This novel methodology not only obviates the need for traditional catalysts but also harnesses the energy of photons to selectively introduce trifluoromethyl groups into indole substrates. Leveraging the inexpensive, easily handled, and non-toxic Langlois reagent (CF3SO2Na) as the CF3 source, in conjunction with visible light and tert-butyl hydrogen peroxide (TBHP), facilitates the direct C─H trifluoromethylation of indoles. The mechanistic pathway of the reaction is predicted with the help of density functional theory (DFT) calculations at the (U)B3LYP/6–31++G(d,p)/SMD/acetonitrile level of theory.

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来源期刊
ChemistrySelect
ChemistrySelect Chemistry-General Chemistry
CiteScore
3.30
自引率
4.80%
发文量
1809
审稿时长
1.6 months
期刊介绍: ChemistrySelect is the latest journal from ChemPubSoc Europe and Wiley-VCH. It offers researchers a quality society-owned journal in which to publish their work in all areas of chemistry. Manuscripts are evaluated by active researchers to ensure they add meaningfully to the scientific literature, and those accepted are processed quickly to ensure rapid online publication.
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